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For both chips, the current profiles did not change with the supply voltage, which suggests linear regulation for both radios.
Although the signal intensity follows the theoretical distribution pattern over a certain range for both chips, there is a marked difference in the valid intensity range between the two chips.
The analysis of the factor loadings (FL, correlation coefficients between original variables and components) of the first 6 PCs revealed that the FLs which better discriminate between permanent AF patients and controls were: FL of the 2nd PC for both chips (namely, FL2A and FL2B); FL of the 3rd component of chip A (FL3A); and FL of the 5th component of chip B (FL5B).
However, glucose yields were very similar for both chips and milled wood for longer pretreatment times.
GenomeStudio v1.7.4 software (Illumina, San Diego, California, USA) was used to detect the SNPs for both chips and both assemblies.
Quality control was performed within-breed on the HD and 50K genotypes, using the same criteria for both chips.
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As a positive control for both ChIP-qPCR and ChIP-seq, labs can look at genomic regions known to bind the protein of interest or use the antibody against histone H3 as a 'universal' positive control, which will, he says, enrich for any genomic locus if the chromatin was intact and the IP worked as planned.
The first principal component is prevailing for both chip platforms.
In contrast, specific signals were reproducibly observed for both ChIP-seq samples.
Single-ended 36-bp reads were generated for both ChIP- and RNA-sequencing runs.
The first principal component is prevailing for both chip platform data.
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